Acetyl chloride → 1-(7-acetyl-4,5-dihydro-1H-1,5-methanobenzo[d]azepin-3(2H)-yl)-2,2,2-trifluoroethanone

HRID 1271344노트

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HRID 1271344 반응식
[CH:1]12[CH2:18][CH:8]([CH2:9][N:10]([C:12](=[O:17])[C:13]([F:16])([F:15])[F:14])[CH2:11]1)[C:7]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]2=1.[C:19](Cl)([CH3:21])=[O:20].[Cl-].[Al+3].[Cl-].[Cl-].C([O-])(O)=O.[Na+]>ClCCCl>[C:19]([C:5]1[CH:4]=[CH:3][C:2]2[CH:1]3[CH2:18][CH:8]([CH2:9][N:10]([C:12](=[O:17])[C:13]([F:15])([F:16])[F:14])[CH2:11]3)[C:7]=2[CH:6]=1)(=[O:20])[CH3:21]

참가 물질

6

실험 절차

1-(10-Aza-tricyclo[6.3.1.02,7]dodeca-2(7),3,5-trien-10-yl)-2,2,2-trifluoro-ethanone (253 mg, 1.0 mmol) and AcCl (0.68 mL, 10 mmol) were dissolved in DCE (3 mL) and treated with aluminum chloride (AlCl3) (667 mg, 5.0 mmol). The resulting yellow mixture was stirred for 30 minutes then poured over ice and saturated aqueous NaHCO3 solution. After stirring 20 minutes the mixture was extracted with CH2Cl2 (3×30 mL). The organic layer was dried through a cotton plug then concentrated to a orange-yellow oil (255 mg, 86%).

후처리

  1. stirringAfter stirring 20 minutes the mixture
  2. extractionwas extracted with CH2Cl2 (3×30 mL)
  3. customThe organic layer was dried through a cotton plug
  4. concentrationthen concentrated to a orange-yellow oil (255 mg, 86%)

출처 및 근거

ORD 기록
ord-ef5879f44237410b9a686d0f48fff154
출처 데이터셋
uspto-grants-2007_04
특허 번호
US07205300B2

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